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rs2274089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs2274089(A;A)
Make rs2274089(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position25488355
GeneLRRC16A
is asnp
is mentioned by
dbSNPrs2274089
ebirs2274089
HLIrs2274089
Exacrs2274089
Varsomers2274089
Maprs2274089
PheGenIrs2274089
hapmaprs2274089
1000 genomesrs2274089
hgdprs2274089
ensemblrs2274089
gopubmedrs2274089
geneviewrs2274089
scholarrs2274089
googlers2274089
pharmgkbrs2274089
gwascentralrs2274089
openSNPrs2274089
23andMers2274089
23andMe allrs2274089
SNP Nexus

SNPshotrs2274089
SNPdbers2274089
MSV3drs2274089
GWAS Ctlgrs2274089
GMAF0.04362
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19084217OA-icon.png]
Trait Serum markers of iron status
Title Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels
Risk Allele
P-val 3E-7
Odds Ratio NR NR





GET Evidence
rs2274089
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary